Canonical Allele Identifier: CA399727801

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.44007683A>T , CM000679.2:g.44007683A>T GRCh38
NC_000017.10:g.42085051A>T , CM000679.1:g.42085051A>T GRCh37
NC_000017.9:g.39440577A>T NCBI36
NG_008106.1:g.8020A>T
NG_023338.1:g.1787T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000293404.8:c.1361A>T (NAGS) MANE Select ENSP00000293404.2:p.Gln454Leu
ENST00000293404.7:c.1361A>T (NAGS) ENSP00000293404.2:p.Gln454Leu
ENST00000589767.1:c.1292A>T (NAGS) ENSP00000465408.1:p.Gln431Leu
ENST00000592915.1:n.1249A>T (NAGS)
NM_153006.2:c.1361A>T (NAGS) NP_694551.1:p.Gln454Leu
XM_011524438.1:c.1268+189A>T (NAGS) XP_011522740.1:n.1268+189A>T
XM_011524439.1:c.863A>T (NAGS) XP_011522741.1:p.Gln288Leu
XM_011525035.1:c.-463+15889T>A (PYY) XP_011523337.1:n.-463+15889T>A
XM_011524439.2:c.863A>T (NAGS) XP_011522741.1:p.Gln288Leu
NM_153006.3:c.1361A>T (NAGS) MANE Select NP_694551.1:p.Gln454Leu